Ruidaton powered airflow floating treatment bed (unsterilized) - Taiwan Registration 951f36b4d06aece24885dd7cb90053b2
Access comprehensive regulatory information for Ruidaton powered airflow floating treatment bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 951f36b4d06aece24885dd7cb90053b2 and manufactured by REDACTRON INTERNATIONAL B.V.. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Airflow Floating Treatment Bed (O.5170)".
o Physical Medical Sciences
O.5170 5170.
import
Dates and Status
Jul 22, 2010
Jul 22, 2015
Apr 25, 2018
Cancellation Information
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